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JPH06891B2 - Aromatic polysulfone resin composition - Google Patents
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JPH06891B2 - Aromatic polysulfone resin composition - Google Patents

Aromatic polysulfone resin composition

Info

Publication number
JPH06891B2
JPH06891B2 JP29458185A JP29458185A JPH06891B2 JP H06891 B2 JPH06891 B2 JP H06891B2 JP 29458185 A JP29458185 A JP 29458185A JP 29458185 A JP29458185 A JP 29458185A JP H06891 B2 JPH06891 B2 JP H06891B2
Authority
JP
Japan
Prior art keywords
weight
aromatic polysulfone
examples
ethylene
ethylene copolymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP29458185A
Other languages
Japanese (ja)
Other versions
JPS62151463A (en
Inventor
眞一 井上
邦明 浅井
靖朗 鈴木
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP29458185A priority Critical patent/JPH06891B2/en
Priority to PCT/JP1987/000444 priority patent/WO1989000182A1/en
Publication of JPS62151463A publication Critical patent/JPS62151463A/en
Publication of JPH06891B2 publication Critical patent/JPH06891B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L81/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
    • C08L81/06Polysulfones; Polyethersulfones

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Description

【発明の詳細な説明】 <産業上の利用分野> 本発明は、優れた衝撃特性を有する芳香族ポリスルフォ
ン樹脂組成物に関する。
TECHNICAL FIELD The present invention relates to an aromatic polysulfone resin composition having excellent impact properties.

<従来技術> 芳香族ポリスルフォンは耐熱性、強度剛性、難燃性、耐
クリープ特性の優れたエンジニアリングプラスチックと
して、昨今の薄肉化、小型化が要求される電気電子部品
や自動車部品およびOA機器部品などの用途において注
目されている。
<Prior Art> Aromatic polysulfone is an engineering plastic excellent in heat resistance, strength and rigidity, flame retardancy, and creep resistance, and electric and electronic parts, automobile parts, and OA equipment parts that are required to be thin and compact these days. It is drawing attention in applications such as.

しかしながら、衝撃強度の面では同等の耐熱性を有する
ポリエーテルイミドやポリフェニレンサルファイドなど
にくらべると高い値を有しているが、ポリカーボネート
やポリアリーレンエステルにくらべると延性に乏しく脆
弱であり該用途面においても制限をうける場合がある。
However, in terms of impact strength, although it has a higher value than polyetherimide or polyphenylene sulfide having equivalent heat resistance, it has poor ductility and is fragile as compared to polycarbonate or polyarylene ester, and in terms of the application aspect. May be subject to restrictions.

<発明が解決しようとする問題点> 本発明では、芳香族ポリスルフォンの耐熱性、剛性を低
下させないで衝撃強度が改良された組成物を提供するこ
とを目的とするものである。
<Problems to be Solved by the Invention> An object of the present invention is to provide a composition having improved impact strength without lowering the heat resistance and rigidity of aromatic polysulfone.

<問題点を解決するための手段> 本発明者は、上記の状況に鑑み、鋭意検討した結果、芳
香族ポリスルフォンにエチレン、α,β−不飽和カルボ
ン酸アルキルエステルおよび無水マレイン酸からなるエ
チレン共重合体を配合することにより、芳香族ポリスル
フォンの耐熱性、剛性を低下させないで、優れた衝撃特
性を有する組成物を得ることができることを見出し、本
発明に達した。
<Means for Solving Problems> The inventors of the present invention have made diligent studies in view of the above situation, and as a result, ethylene containing an aromatic polysulfone, an α, β-unsaturated carboxylic acid alkyl ester, and maleic anhydride was used. The present inventors have found that a composition having excellent impact properties can be obtained without reducing the heat resistance and rigidity of the aromatic polysulfone by blending the copolymer, and have reached the present invention.

すなわち、本発明は(A)芳香族ポリスルフォン70〜9
9重量%および(B)エチレン50〜90重量%、α,β
−不飽和カルボン酸アルキルエステル5〜49重量%お
よび無水マレイン酸0.5〜10重量%からなるエチレン
共重合体30〜1重量%からなることを特徴とする樹脂
組成物である。
That is, the present invention relates to (A) aromatic polysulfone 70 to 9
9% by weight and (B) ethylene 50 to 90% by weight, α, β
A resin composition comprising an ethylene copolymer of 5 to 49% by weight and an ethylene copolymer of 0.5 to 10% by weight and an ethylene copolymer of 30 to 1% by weight.

本発明組成物の成分として使用される芳香族ポリスルフ
ォンはアリーレン単位がエーテルおよびスルフォン結合
と共に無秩序にまたは秩序正しく位置するポリアリーレ
ン化合物として定義される。たとえば、つぎの(1)〜(1
6)のような構造式からなるものがあげられるが、とくに
(1),(2),(6)の構造を有するものが物性と加工性のバ
ランスがすぐれており好ましい。
The aromatic polysulfone used as a component of the composition of the present invention is defined as a polyarylene compound in which the arylene units are randomly or ordered with ether and sulfone bonds. For example, the following (1) ~ (1
There are those consisting of structural formulas such as 6), but especially
Those having the structures (1), (2), and (6) are preferable because they have a good balance of physical properties and workability.

さらに、溶液100cc中に重合体1gを含むジメチルフ
ォルムアミド溶液について、25℃で測定された還元粘
度が0.3以上0.6以下の時、該芳香族ポリスルフォンの耐
熱性、強度、剛性、靭性などの物性と成形加工性のバラ
ンスがすぐれており、より好ましい。
Furthermore, when the reduced viscosity measured at 25 ° C. is 0.3 or more and 0.6 or less for a dimethylformamide solution containing 1 g of the polymer in 100 cc of the solution, the aromatic polysulfone has physical properties such as heat resistance, strength, rigidity and toughness. It is more preferable because it has a good balance of molding processability.

本発明で用いられるエチレン共重合体は、その単量体成
分が、エチレン、α、β−不飽和カルボン酸アルキルエ
ステル、および無水マレイン酸から成り、エチレンが5
0〜90重量%、好ましくは60〜85重量%、α、β
−不飽和カルボン酸アルキルエステルが5〜49重量
%、好ましくは7〜45重量%、および無水マレイン酸
が0.5〜10重量%、好ましくは1〜8重量%である。
The ethylene copolymer used in the present invention has a monomer component composed of ethylene, an α, β-unsaturated carboxylic acid alkyl ester, and maleic anhydride, wherein ethylene is 5
0 to 90% by weight, preferably 60 to 85% by weight, α, β
5 to 49% by weight, preferably 7 to 45% by weight of unsaturated carboxylic acid alkyl esters, and 0.5 to 10% by weight, preferably 1 to 8% by weight of maleic anhydride.

α,β−不飽和カルボン酸アルキルエステルは、炭素数
が3〜8個の不飽和カルボン酸、例えば、アクリル酸、
メタクリル酸などのアルキルエステルであって、具体例
としては、アクリル酸メチル、アクリル酸エチル、アク
リル酸n−プロピル、アクリル酸イソプロピル、アクリ
ル酸n−ブチル、アクリル酸t−ブチル、アクリル酸イ
ソブチル、メタクリル酸メチル、メタクリル酸エチル、
メタクリル酸n−プロピル、メタクリル酸イソプロピ
ル、メタクリル酸n−ブチル、メタクリル酸t−ブチ
ル、およびメタクリル酸イソブチルなどがあり、これら
のうちでも特に、アクリル酸エチル、アクリル酸n−ブ
チル、メタクリル酸メチルが好ましい。
The α, β-unsaturated carboxylic acid alkyl ester is an unsaturated carboxylic acid having 3 to 8 carbon atoms, for example, acrylic acid,
An alkyl ester such as methacrylic acid, and specific examples thereof include methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, t-butyl acrylate, isobutyl acrylate, methacrylic acid. Methyl acid, ethyl methacrylate,
There are n-propyl methacrylate, isopropyl methacrylate, n-butyl methacrylate, t-butyl methacrylate, isobutyl methacrylate, and the like. Among these, ethyl acrylate, n-butyl acrylate, and methyl methacrylate are particularly preferable. preferable.

これらエチレン共重合体を芳香族ポリスルフォンへ配合
する量は、芳香族ポリスルフォンと該エチレン共重合体
の合計量に対して、芳香族ポリスルフォン70〜99重
量%、エチレン共重合体80〜1重量%が適当であり、
芳香族ポリスルフォンが99重量%を越え、該エチレン
共重合体が1重量%未満の場合には目的とする衝撃強度
を改良する効果が不十分でまた芳香族ポリスルフォンが
70重量%未満、該エチレン共重合体が80重量%を越
えた場合には、芳香族ポリスルフォンの特徴である耐熱
性と剛性の低下が著しく好ましくない。
The amount of the ethylene copolymer to be blended with the aromatic polysulfone is 70 to 99% by weight of the aromatic polysulfone and 80 to 1% of the ethylene copolymer based on the total amount of the aromatic polysulfone and the ethylene copolymer. Wt% is appropriate,
When the amount of aromatic polysulfone exceeds 99% by weight and the amount of the ethylene copolymer is less than 1% by weight, the effect of improving the desired impact strength is insufficient, and the amount of aromatic polysulfone is less than 70% by weight. When the ethylene copolymer exceeds 80% by weight, the heat resistance and the rigidity, which are the characteristics of the aromatic polysulfone, are significantly lowered, which is not preferable.

本発明の組成物の配合手段は特に限定されない。The compounding means of the composition of the present invention is not particularly limited.

各々別々に溶融混合機に供給することが可能であり、ま
たあらかじめこれら原料類を乳鉢、ヘンシェルミキサ
ー、ボールミル、リポンブレンダーなどを利用して予備
混合してから溶融混合機に供給することもできる。
It is possible to supply them separately to the melt mixer, or it is possible to pre-mix these raw materials using a mortar, a Henschel mixer, a ball mill, a repon blender, etc. before supplying them to the melt mixer.

なお、本発明組成物に対して、本発明の目的をそこなわ
ない範囲で、酸化防止剤および熱安定剤、紫外線吸収
剤、滑剤、離型剤、染料、顔料などの着色剤、難燃剤、
難燃助剤、帯電防止剤などの通常の添加剤を1種以上添
加することができる。
Incidentally, with respect to the composition of the present invention, within a range that does not impair the object of the present invention, antioxidants and heat stabilizers, ultraviolet absorbers, lubricants, release agents, dyes, colorants such as pigments, flame retardants,
One or more conventional additives such as flame retardant aids and antistatic agents can be added.

また、少量の他の熱可塑性樹脂(例えばポリエチレン、
ポリプロピレン、ポリアミド、ポリカーボネート、ポリ
アリーレンエステル、変性ポリフェニレンオキサイド、
など)、熱硬化性樹脂(例えばフェノール樹脂、エポキ
シ樹脂など)を1種以上添加することができる。
Also, small amounts of other thermoplastics (eg polyethylene,
Polypropylene, polyamide, polycarbonate, polyarylene ester, modified polyphenylene oxide,
Etc.), and one or more thermosetting resins (for example, phenol resin, epoxy resin, etc.) can be added.

さらに、ガラス繊維、カーボン繊維、ボロン繊維、炭化
ケイ素繊維、アスベスト繊維、金属繊維などの補強剤、
クレー、マイカ、シリカ、グラファイト、ガラスビー
ズ、アルミナ、炭酸カルシウムなどの充填剤を配合する
ことも可能である。
Furthermore, reinforcing agents such as glass fiber, carbon fiber, boron fiber, silicon carbide fiber, asbestos fiber and metal fiber,
It is also possible to blend a filler such as clay, mica, silica, graphite, glass beads, alumina and calcium carbonate.

特に、ガラス繊維またはカーボン繊維はその充填による
剛性度の向上、耐熱性の向上効果が顕著であり、より有
用な組成物を提供するため、全組成物に対して10〜6
0wt%の範囲で充填することが好ましい。該繊維は直径
5〜15μで長さ3〜8mmの単繊維を数百〜数千本集束
したチョップドストランドやチョップドファイバーもし
くは長繊維であるロービングを用い、最終組成物中に平
均繊維長が0.15〜0.5mmの範囲となるよう均一に分散さ
せることが好ましい。
In particular, glass fiber or carbon fiber has a remarkable effect of improving rigidity and heat resistance due to the filling thereof, and in order to provide a more useful composition, 10 to 6 relative to the entire composition.
It is preferable to fill in the range of 0 wt%. The fibers used are chopped strands or chopped fibers obtained by bundling hundreds to thousands of single fibers having a diameter of 5 to 15 μm and a length of 3 to 8 mm, or rovings which are long fibers, and the average fiber length in the final composition is 0.15 to It is preferable to disperse uniformly so as to be in the range of 0.5 mm.

以下、実施例により本発明を説明するが、これらは単な
る例示であり、本発明はこれに限定されることはない。
Hereinafter, the present invention will be described with reference to examples, but these are merely examples and the present invention is not limited thereto.

実施例1〜8 基本構造として を有するポリエーテルスルフォン(ICI製ポリエーテ
ルスルフォン8600P)とエチレン67%、アクリル
酸エチル30.5%および無水マレイン酸2.5%からなるエ
チレン共重合体を第1表に示した組成で混合し、二軸押
出機(池貝鉄工製PCM−30)により、330℃の温
度で溶融混練した後、ストランドを氷冷、切断してペレ
ットを得た。
Examples 1 to 8 As a basic structure A poly (ethylene sulfone 8600P manufactured by ICI) and an ethylene copolymer consisting of 67% of ethylene, 30.5% of ethyl acrylate and 2.5% of maleic anhydride were mixed in a composition shown in Table 1 and then biaxially extruded. Using a machine (PCM-30 manufactured by Ikegai Tekko Co., Ltd.), after melt-kneading at a temperature of 330 ° C., the strands were ice-cooled and cut to obtain pellets.

得られたペレットを射出成形し(住友重機−ネスタール
47/28射出成形機、シリンダー温度340〜360
℃、金型温度180℃)、アイゾット衝撃強度試験片、
曲げ試験片、熱変形温度測定試験片を得た。
The obtained pellets were injection molded (Sumitomo Heavy Industries-Nestal
47/28 injection molding machine, cylinder temperature 340-360
℃, mold temperature 180 ℃), Izod impact strength test piece,
Bending test pieces and heat distortion temperature measurement test pieces were obtained.

それぞれASTM D−256、D−790、D−64
8に従って測定した。(結果を第1表に示す)いずれも
すぐれた値が得られている。
ASTM D-256, D-790, D-64 respectively
It measured according to 8. (Results are shown in Table 1) Excellent values were obtained in all cases.

比較例1〜2 実施例1〜3に用いた芳香族ポリスルフォンとエチレン
共重合体を第1表に示した割合で混合し、実施例1〜3
と同様の加工を行い、物性を測定した。(結果を第1表
に示す)実施例に比較して著しく劣っている。
Comparative Examples 1 to 2 The aromatic polysulfone used in Examples 1 to 3 and the ethylene copolymer were mixed in the proportions shown in Table 1 to give Examples 1 to 3.
The same processing was performed and the physical properties were measured. (Results are shown in Table 1) Remarkably inferior to the examples.

実施例4〜6 基本構造として を有するポリスルフォン(UCC社製、Udelp170
0)と実施例1〜3で用いたエチレン共重合体を第2表
に示した組成で混合し、実施例1〜3と同様の方法によ
りペレット化し、射出成形により、アイゾット衝撃強度
試験片、曲げ試験片、熱変形温度測定試験片を得、測定
に供した。
Examples 4 to 6 As basic structure Polysulfone with UCC (Udelp170
0) and the ethylene copolymers used in Examples 1 to 3 were mixed in a composition shown in Table 2, pelletized by the same method as in Examples 1 to 3, and injection molded to obtain Izod impact strength test pieces. Bending test pieces and heat distortion temperature measurement test pieces were obtained and provided for measurement.

なおこの時の押出時の温度は300℃、射出成形はシリ
ンダー温度330〜350℃、金型温度130℃で行な
った。
At this time, the extrusion temperature was 300 ° C., the injection molding was performed at a cylinder temperature of 330 to 350 ° C., and the mold temperature was 130 ° C.

結果を第2表に示す。The results are shown in Table 2.

比較例3〜4 実施例4〜6に用いたポリスルフォンとエチレン共重合
体を第2表に示した割合で混合し、実施例4〜6と同様
の加工を行ない物性を測定した。
Comparative Examples 3 to 4 The polysulfone used in Examples 4 to 6 and the ethylene copolymer were mixed in the proportions shown in Table 2, and the same processing as in Examples 4 to 6 was performed to measure the physical properties.

結果を第2表に示す。実施例に比較して著しく劣ってい
る。
The results are shown in Table 2. It is significantly inferior to the examples.

実施例7〜8 実施例1〜3と同じ構造を有するポリエーテルスルフォ
ン、エチレン75.5%、アクリル酸エチル22.5%および無
水マレイン酸2.0%からなるエチレン共重合体およびガ
ラス繊維(旭ファイバーグラス社製CS03−MA49
7、長さ3mmのチョップドストランド)を第3表に示し
た組成で混合し、二軸押出機(池貝鉄工製PCM−3
0)により、340℃の温度で、溶融混練した後、スト
ランドを水冷、切断してペレットを得た。
Examples 7 to 8 Polyethylene sulfone having the same structure as in Examples 1 to 3, ethylene 75.5%, ethylene copolymer consisting of ethyl acrylate 22.5% and maleic anhydride 2.0%, and glass fiber (CS03 manufactured by Asahi Fiber Glass Co., Ltd.). -MA49
7, chopped strands with a length of 3 mm) were mixed in the composition shown in Table 3 and a twin-screw extruder (PCM-3 manufactured by Ikegai Tekko Co., Ltd.) was mixed.
According to 0), after melt-kneading at a temperature of 340 ° C., the strand was water-cooled and cut to obtain pellets.

得られたペレットを射出成形し(住友重機−ネスタール
47/28射出成形機、シリンダー温度350℃、金型温度
130℃)、アイゾット衝撃試験片、曲げ試験片、熱変
形温度測定用試験片を得た。それぞれASTM D−2
56、D−790、D−648に従って測定した。
The obtained pellets were injection molded (Sumitomo Heavy Industries-Nestal
47/28 injection molding machine, cylinder temperature 350 ° C., mold temperature 130 ° C.), Izod impact test piece, bending test piece, and test piece for measuring heat distortion temperature were obtained. Each ASTM D-2
56, D-790, D-648.

結果を第3表に示す。The results are shown in Table 3.

比較例5 実施例7〜8に用いたポリエーテルスルフォンとガラス
繊維を第3表に示した割合で混合し、実施例7〜8と同
様の加工を行い、物性を測定した。(結果を第3表に示
す。)実施例に比較して著しく劣っている。
Comparative Example 5 The polyether sulfone used in Examples 7 to 8 and glass fiber were mixed in the proportions shown in Table 3, the same processing as in Examples 7 to 8 was performed, and the physical properties were measured. (The results are shown in Table 3.) Remarkably inferior to the examples.

<発明の効果> 本発明の芳香族ポリフルフォン樹脂にエチレン、α,β
−不飽和カルボン酸アルキルエステルおよび無水マレイ
ン酸からなるエチレン共重合体を配合した組成物は芳香
族ポリスルフォン樹脂の耐熱性、剛性を低下させない
で、衝撃強度が顕著に改良されたものである。
<Effect of the Invention> Ethylene, α, β are added to the aromatic polyflufon resin of the present invention.
A composition containing an ethylene copolymer composed of an unsaturated carboxylic acid alkyl ester and maleic anhydride has a markedly improved impact strength without lowering the heat resistance and rigidity of the aromatic polysulfone resin.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】(A)芳香族ポリスルフォン70〜99重量
%および (B)エチレン50〜90重量%、α,β−不飽和カルボ
ン酸アルキルエステル5〜49重量%および無水マレイ
ン酸0.5〜10重量%からなるエチレン共重合体30〜
1重量% からなることを特徴とする樹脂組成物。
1. (A) 70 to 99% by weight of aromatic polysulfone and (B) 50 to 90% by weight of ethylene, 5 to 49% by weight of α, β-unsaturated carboxylic acid alkyl ester and 0.5 to 10 of maleic anhydride. Ethylene copolymer 30% by weight
A resin composition comprising 1% by weight.
JP29458185A 1985-12-26 1985-12-26 Aromatic polysulfone resin composition Expired - Lifetime JPH06891B2 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
JP29458185A JPH06891B2 (en) 1985-12-26 1985-12-26 Aromatic polysulfone resin composition
PCT/JP1987/000444 WO1989000182A1 (en) 1985-12-26 1987-06-30 Aromatic polysulfone resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29458185A JPH06891B2 (en) 1985-12-26 1985-12-26 Aromatic polysulfone resin composition

Publications (2)

Publication Number Publication Date
JPS62151463A JPS62151463A (en) 1987-07-06
JPH06891B2 true JPH06891B2 (en) 1994-01-05

Family

ID=17809631

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29458185A Expired - Lifetime JPH06891B2 (en) 1985-12-26 1985-12-26 Aromatic polysulfone resin composition

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JP (1) JPH06891B2 (en)
WO (1) WO1989000182A1 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06892B2 (en) * 1987-05-14 1994-01-05 住友ダウ株式会社 Thermoplastic resin composition
KR100625072B1 (en) 2002-01-29 2006-09-19 가부시키가이샤 제이텍트 Electric power steering system

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4360636A (en) * 1981-07-27 1982-11-23 Stauffer Chemical Company Blends of a sulfone polymer and impact resistant interpolymer

Also Published As

Publication number Publication date
JPS62151463A (en) 1987-07-06
WO1989000182A1 (en) 1989-01-12

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